Mortality trends in idiopathic pulmonary fibrosis in Europe between 2013 and 2018.

<bold>Objective:</bold> To provide contemporary estimates of IPF mortality rates across 24 European Countries from 2013 to 2018, using death certificates data from the European Statistics Institution (EUROSTAT) database. <bold>Methods:</bold> We extracted country data for IPF (International Classification of Diseases 10th Edition, ICD-10, code “J84.1”) mortality from the EUROSTAT dataset. We calculated country- age- and sex-specific death registration rates between 2013 and 2018. We used direct standardisation to compare rates between countries. <bold>Results:</bold> The overall standardised mortality rate in EU Countries during this period was 3.90 per 100000 person-years (95%, CI 3.80-3.90), with the rate raising from 3.70 in the 2013 to 4.00 in the 2018. We observed substantial inter-country differences, with the highest rates detected in Ireland, the UK, and Finland, the lowest rate in Bulgaria, and middle rates in Germany, Greece, Italy, the Netherlands, Portugal, and Slovenia (Fig 1). <bold>Conclusion:</bold> There are currently more than 17,000 deaths recorded from IPF each year in Europe but the marked geographical differences we observed suggest that this figure may underestimate the true rate considerably.

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Journal
Epidemiology
Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa494
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
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article

Mortality trends in idiopathic pulmonary fibrosis in Europe between 2013 and 2018.

Martina Bonifazi, Francesca Gonnelli, Richard Hubbard
Epidemiology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Mortality trends in idiopathic pulmonary fibrosis in Europe between 2013 and 2018.

Martina Bonifazi, Francesca Gonnelli, Richard Hubbard
article en

Abstract

<bold>Objective:</bold> To provide contemporary estimates of IPF mortality rates across 24 European Countries from 2013 to 2018, using death certificates data from the European Statistics Institution (EUROSTAT) database. <bold>Methods:</bold> We extracted country data for IPF (International Classification of Diseases 10th Edition, ICD-10, code “J84.1”) mortality from the EUROSTAT dataset. We calculated country- age- and sex-specific death registration rates between 2013 and 2018. We used direct standardisation to compare rates between countries. <bold>Results:</bold> The overall standardised mortality rate in EU Countries during this period was 3.90 per 100000 person-years (95%, CI 3.80-3.90), with the rate raising from 3.70 in the 2013 to 4.00 in the 2018. We observed substantial inter-country differences, with the highest rates detected in Ireland, the UK, and Finland, the lowest rate in Bulgaria, and middle rates in Germany, Greece, Italy, the Netherlands, Portugal, and Slovenia (Fig 1). <bold>Conclusion:</bold> There are currently more than 17,000 deaths recorded from IPF each year in Europe but the marked geographical differences we observed suggest that this figure may underestimate the true rate considerably.

Epidemiology
Marche Polytechnic University (IT), University of Nottingham (GB)
Good health and well-being
Openalex Percentile: Top 62%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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Mortality trends in idiopathic pulmonary fibrosis in Europe between 2013 and 2018. — Martina Bonifazi, Francesca Gonnelli, et al. · Epidemiology (2024) | TGRS Research Map | TGRS